Tetrapyrroles and derivatives
Cobalt(II) phthalocyanine
CAS: 3317-67-7 Molecular Formula: C32H16CoN8 Molecular Weight (g/mol): 571.469 MDL Number: MFCD00010718 InChI Key: MPMSMUBQXQALQI-UHFFFAOYSA-N Synonym: cobalt ii phthalocyanine,cobalt phthalocyanine,phthalocyanine cobalt ii,phthalocyanine, cobalt,cobalt ii phthalocyanine, beta-form, dye content 97 % PubChem CID: 2734991 SMILES: C1=CC=C2C(=C1)C3=NC4=NC(=NC5=C6C=CC=CC6=C([N-]5)N=C7C8=CC=CC=C8C(=N7)N=C2[N-]3)C9=CC=CC=C94.[Co+2]
Cobalt(II) Phthalocyanine 93.0+%, TCI America™
CAS: 3317-67-7 Molecular Formula: C32H16CoN8 Molecular Weight (g/mol): 571.469 MDL Number: MFCD00010718 InChI Key: MPMSMUBQXQALQI-UHFFFAOYSA-N Synonym: cobalt ii phthalocyanine,cobalt phthalocyanine,phthalocyanine cobalt ii,phthalocyanine, cobalt,cobalt ii phthalocyanine, beta-form, dye content 97 % PubChem CID: 2734991 SMILES: C1=CC=C2C(=C1)C3=NC4=NC(=NC5=C6C=CC=CC6=C([N-]5)N=C7C8=CC=CC=C8C(=N7)N=C2[N-]3)C9=CC=CC=C94.[Co+2]
Vitamin B12, MP Biomedicals™
CAS: 68-19-9 Molecular Formula: C63H88CoN14O14P Molecular Weight (g/mol): 1355.39 MDL Number: MFCD00151092 InChI Key: YUWVGNQGDAPKCX-BVWPOUIRNA-L Synonym: vitamin b12 PubChem CID: 129893524 IUPAC Name: (10S,12R,13R,24S,35R,41R)-30,35,40-tris(2-carbamoylethyl)-24,36,41-tris(carbamoylmethyl)-1-cyano-46-hydroxy-12-(hydroxymethyl)-5,6,17,23,28,31,31,36,38,41,42-undecamethyl-15,20-dioxo-11,14,16-trioxa-2λ⁵,9,19,26λ⁵,43,44λ⁵,45λ⁵-heptaaza-15λ⁵-phospha-1-cobaltadodecacyclo[27.14.1.1¹,³⁴.1²,⁹.1¹⁰,¹³.0¹,²⁶.0³,⁸.0²³,²⁷.0²⁵,⁴².0³²,⁴⁴.0³⁹,⁴³.0³⁷,⁴⁵]heptatetraconta-2(47),3,5,7,26,28,32(44),33,37(45),38-decaene-1,2,26,44,45-pentakis(ylium)-15-olate SMILES: [C@@H]1(C2=CC3=[N+]4C(C(C3(C)C)CCC(N)=O)=C(C3=[N+]5C6C7(N8C(C([C@@]7(C)CC(N)=O)CCC(N)=O)=C(C(=[N+]2[Co+]458([N+]2=CN(C4=CC(=C(C)C=C24)C)[C@@]2([H])O[C@@H]([C@]([H])(OP([O-])(=O)OC(C)CNC(=O)CCC3(C)[C@@H]6CC(N)=O)C2O)CO)C#N)C1(C)CC(N)=O)C)C)C)CCC(N)=O
Vitamin B12, 98+% (dry wt basis)
CAS: 68-19-9 Molecular Formula: C63H88CoN14O14P Molecular Weight (g/mol): 1355.39 MDL Number: MFCD00151092 InChI Key: YUWVGNQGDAPKCX-BVWPOUIRNA-L Synonym: vitamin b12 PubChem CID: 129893524 IUPAC Name: cobalt(2+);[(2R,3S,4R,5S)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2R)-1-[3-[(1R,2R,3R,5Z,7S,10Z,12S,13S,15Z,17S,18S,19R)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl- SMILES: [C@@H]1(C2=CC3=[N+]4C(C(C3(C)C)CCC(N)=O)=C(C3=[N+]5C6C7(N8C(C([C@@]7(C)CC(N)=O)CCC(N)=O)=C(C(=[N+]2[Co+]458([N+]2=CN(C4=CC(=C(C)C=C24)C)[C@@]2([H])O[C@@H]([C@]([H])(OP([O-])(=O)OC(C)CNC(=O)CCC3(C)[C@@H]6CC(N)=O)C2O)CO)C#N)C1(C)CC(N)=O)C)C)C)CCC(N)=O
Thermo Scientific Chemicals Cyanocobalamin, 96%
CAS: 68-19-9 Molecular Formula: C63H88CoN14O14P Molecular Weight (g/mol): 1355.39 MDL Number: MFCD00151092 InChI Key: YUWVGNQGDAPKCX-BVWPOUIRNA-L Synonym: vitamin b12 PubChem CID: 129893524 IUPAC Name: cobalt(2+);[(2R,3S,4R,5S)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2R)-1-[3-[(1R,2R,3R,5Z,7S,10Z,12S,13S,15Z,17S,18S,19R)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl- SMILES: [C@@H]1(C2=CC3=[N+]4C(C(C3(C)C)CCC(N)=O)=C(C3=[N+]5C6C7(N8C(C([C@@]7(C)CC(N)=O)CCC(N)=O)=C(C(=[N+]2[Co+]458([N+]2=CN(C4=CC(=C(C)C=C24)C)[C@@]2([H])O[C@@H]([C@]([H])(OP([O-])(=O)OC(C)CNC(=O)CCC3(C)[C@@H]6CC(N)=O)C2O)CO)C#N)C1(C)CC(N)=O)C)C)C)CCC(N)=O
Cayman Chemical CobaltIc III ProtoporphyrIn
An inducer of HO-1 activity; induces HO-1 activity in vitro and in vivo; reduces δ-aminolevulinate synthase and CYP activities in rat liver microsomes ex vivo at 125 µmol/kg; prevents liver injury and increases in the percentage of hepatic apoptotic cells in a mouse model of liver ischemia-reperfusion injury at 5 mg/kg; increases survival and decreases the number of lung CFUs in mice infected with Y. pestis; has also been used as a catalyst for the electrochemical reduction of carbon dioxide in carbon electrodes
Medchemexpress LLC Cobalt phthalocyanine | 3317-67-7 | 98.0% | 571.46 | 10 G
Cobalt phthalocyanine is identified as a catalyst for redox reactions. It specifically catalyzes the aerobic regeneration of aldehydes and ketones from their corresponding aldoximes and ketoximes. This compound also finds application in the development of electrocatalysts.
- Catalyst of redox reaction
- Catalyzes aerobic regenerations of aldehydes and ketones from aldoximes and ketoximes
- Can be used in the development of electrocatalysts
- Capable of reducing CO2 to CO in water with high activity over a broad pH range from 4 to 14
Medchemexpress LLC Cobalt phthalocyanine | 3317-67-7 | 98.0% | 571.46 | 1 G
Cobalt phthalocyanine acts as a catalyst in redox reactions, specifically facilitating the aerobic regeneration of aldehydes and ketones from aldoximes and ketoximes. It is also suitable for use in the development of electrocatalysts. This compound has demonstrated the ability to reduce carbon dioxide to carbon monoxide with high activity across a broad pH range, from 4 to 14.
- Catalyzes aerobic regeneration of carbonyl compounds.
- Aids in the development of electrocatalysts.
- Effective in reducing carbon dioxide to carbon monoxide.
- Maintains high activity over a wide pH range.
Fisher Science Education™ 1,6-Hexamethylenediamine, 0.5M Solution
CAS: 102601-60-5 Molecular Formula: C34H32ClCoN4O4 Molecular Weight (g/mol): 655.037 InChI Key: WWNXKQFLDNSNDN-UHFFFAOYSA-K Synonym: cobaltic protoporphyrin ix chloride,3-18-2-carboxyethyl-7,12-bis ethenyl-3,8,13,17-tetramethylporphyrin-21,23-diid-2-yl propanoic acid;chlorocobalt 2+ \n3-18-2-carboxyethyl-7,12-bis ethenyl-3,8,13,17-tetramethylporphyrin-21,23-diid-2-yl propanoic acid;chlorocobalt 2+,3-18-2-carboxyethyl-8,13-bis ethenyl-3,7,12,17-tetramethylporphyrin-21,23-diid-2-yl propanoic acid; chlorocobalt 2+ PubChem CID: 50910263 IUPAC Name: 3-[18-(2-carboxyethyl)-8,13-bis(ethenyl)-3,7,12,17-tetramethylporphyrin-21,24-diid-2-yl]propanoic acid;chlorocobalt(2+) SMILES: CC1=C(C2=CC3=C(C(=C([N-]3)C=C4C(=C(C(=N4)C=C5C(=C(C(=N5)C=C1[N-]2)C=C)C)C=C)C)C)CCC(=O)O)CCC(=O)O.Cl[Co+2]
Medchemexpress LLC Methylcobalamin | 13422-55-4 | 99.0% | 1 ML
Methylcobalamin, a cobalamin and form of vitamin B12, is characterized by a methyl group replacing the cyanide found in cyanocobalamin. This compound features an octahedral cobalt(III) centre and is known for its rare metal-alkyl bonds. Physiologically, it functions as vitamin B12, addressing deficiencies such as pernicious anemia, and is also applied in treating peripheral neuropathy, diabetic neuropathy, and amyotrophic lateral sclerosis.
- Form of vitamin B12 (cobalamin)
- Contains a methyl group instead of cyanide
- Features an octahedral cobalt(III) centre and metal-alkyl bonds
- Equivalent to vitamin B12 for treating deficiencies (e.g., pernicious anemia)
- Used in peripheral neuropathy, diabetic neuropathy, and amyotrophic lateral sclerosis treatment
Medchemexpress LLC Methylcobalamin | 13422-55-4 | 99.0% | 100 MG
Methylcobalamin is a form of vitamin B12, where a methyl group replaces cyanide. It features an octahedral cobalt(III) center and can be obtained as bright red crystals. Notable for containing metal-alkyl bonds, it is physiologically equivalent to vitamin B12. Methylcobalamin is used to treat conditions from vitamin B12 deficiency, including pernicious anemia, peripheral neuropathy, and diabetic neuropathy, and as an initial treatment for amyotrophic lateral sclerosis.
- Form of vitamin B12
- Features an octahedral cobalt(III) center
- Can be obtained as bright red crystals
- Contains metal-alkyl bonds
- Treats vitamin B12 deficiency
- Used for pernicious anemia
- Treats peripheral neuropathy
- Treats diabetic neuropathy
- Initial treatment for amyotrophic lateral sclerosis
- Classified as a human endogenous metabolite
Apexbio Technology LLC Methylcobalamin 13422-55-4 500mg
Methylcobalamin (CAS 13422-55-4) is a biologically active form of vitamin B12 featuring a methyl group as the ligand to the cobalt ion within the cobalamin structure Functioning as a coenzyme for methionine synthase it facilitates the remethylation of homocysteine to methionine an essential step in methylation metabolism and nucleic acid synthesis Due to its direct involvement in methyl group transfers methylcobalamin is widely utilized in biomedical research to investigate cellular methylation processes nervous system function and disorders related to vitamin B12 deficiency
Apexbio Technology LLC Methylcobalamin 13422-55-4 100mg
Methylcobalamin (CAS 13422-55-4) is a biologically active form of vitamin B12 featuring a methyl group as the ligand to the cobalt ion within the cobalamin structure Functioning as a coenzyme for methionine synthase it facilitates the remethylation of homocysteine to methionine an essential step in methylation metabolism and nucleic acid synthesis Due to its direct involvement in methyl group transfers methylcobalamin is widely utilized in biomedical research to investigate cellular methylation processes nervous system function and disorders related to vitamin B12 deficiency
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